《Electrochemical C-H Cyanation of Electron-Rich (Hetero)Arenes》 was published in Chemistry – A European Journal in 2018. These research results belong to Hayrapetyan, Davit; Rit, Raja K.; Kratz, Markus; Tschulik, Kristina; Goossen, Lukas J.. Recommanded Product: 53005-44-0 The article mentions the following:
A straightforward method for the electrochem. C-H cyanation of arenes and heteroarenes that proceeds at room temperature in MeOH, with NaCN as the reagent in a simple, open, undivided electrochem. cell to afford aryl nitriles was reported. The platinum electrodes were passivated by adsorbed cyanide, which allowed conversion of an exceptionally broad range of electron-rich substrates all the way down to dialkyl arenes. The cyanide electrolyte could be replenished with HCN, opening opportunities for salt-free industrial C-H cyanation. In the part of experimental materials, we found many familiar compounds, such as 2-Methoxy-6-methylbenzonitrile(cas: 53005-44-0Recommanded Product: 53005-44-0)
2-Methoxy-6-methylbenzonitrile(cas: 53005-44-0) belongs to nitriles. Nitriles are found in many useful compounds. Nitrile rubber is also widely used as automotive and other seals since it is resistant to fuels and oils. Organic compounds containing multiple nitrile groups are known as cyanocarbons.Recommanded Product: 53005-44-0
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts